Evaluation of thrombin generating capacity in plasma from patients with haemophilia A and B

被引:284
作者
Dargaud, Y
Béguin, S
Lienhart, A
Al Dieri, R
Trzeciak, C
Bordet, JC
Hemker, HC
Negrier, C
机构
[1] Hop Edouard Herriot, Hemostase Lab, F-69003 Lyon, France
[2] Univ Maastricht, Synapse Bv, Cardiovasc Res Inst, Maastricht, Netherlands
关键词
factor VIII; factor IX; haemophilia; thrombin generation;
D O I
10.1160/TH04-10-0706
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In haemophilia patients, a relationship is usually observed between the clinical expression of the disease and plasmatic factor VIII/factor IX (FVIII/FIX) activity. However, it is known from clinical experience, that some haemophilia patients, despite similar FVIII/FIX plasma levels, could exhibit different bleeding phenotype. After determining preanalytical test conditions, we evaluated the thrombin generation capacity from haemophilia plasma samples in various conditions and the potential usefulness of thrombin generation test (TGT) in haemophilia patients. In a series of 46 haemophilia patients (34 haemophiliaA and 12 haemophilia B patients), we found a significant correlation between plasmatic FVIII/FIX levels and endogenous thrombin potential (ETP), peak and time to peak obtained by thrombin generation measurement. In addition, a correlation was found between severe clinical bleeding phenotype and ETP. Our results suggest that TGT could be a promising tool to evaluate haemostasis capacity in patients with haemophilia. Our ex vivo results, obtained 24 hours after FVIII concentrate administration, showed that in patients presenting similar plasmatic FVIIII levels, thrombin generation capacity may be significantly different. These results suggest that in patients with haemophilia, TGT could be useful for individually tailoring prophylactic regimens as well as for adapting clotting factors infusions in surgical situations, in addition to FVIII/FIX plasma clotting activities.
引用
收藏
页码:475 / 480
页数:6
相关论文
共 23 条
  • [1] The thrombogram in rare inherited coagulation disorders:: Its relation to clinical bleeding
    Al Dieri, R
    Peyvandi, F
    Santagostino, E
    Giansily, M
    Mannucci, PM
    Schved, JF
    Béguin, S
    Hemker, HC
    [J]. THROMBOSIS AND HAEMOSTASIS, 2002, 88 (04) : 576 - 582
  • [2] MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C
    BERTINA, RM
    KOELEMAN, BPC
    KOSTER, T
    ROSENDAAL, FR
    DIRVEN, RJ
    DERONDE, H
    VANDERVELDEN, PA
    REITSMA, PH
    [J]. NATURE, 1994, 369 (6475) : 64 - 67
  • [3] Chantarangkul V, 2003, HAEMATOLOGICA, V88, P547
  • [4] Curvers J, 2002, THROMB HAEMOSTASIS, V88, P5
  • [5] DACOSTA A, 1994, THERAPIE, V49, P355
  • [6] FAMILIAL THROMBOPHILIA DUE TO A PREVIOUSLY UNRECOGNIZED MECHANISM CHARACTERIZED BY POOR ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C - PREDICTION OF A COFACTOR TO ACTIVATED PROTEIN-C
    DAHLBACK, B
    CARLSSON, M
    SVENSSON, PJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) : 1004 - 1008
  • [7] Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one-stage assay
    Ghosh, K
    Shetty, S
    Mohanty, D
    [J]. HAEMOPHILIA, 2001, 7 (01) : 9 - 12
  • [8] Thrombin generation measurement in factor VII-depleted plasmas compared to inherited factor VII-deficient plasmas
    Giansily-Blaizot, M
    Al Dieri, R
    Schved, JF
    [J]. PATHOPHYSIOLOGY OF HAEMOSTASIS AND THROMBOSIS, 2003, 33 (01) : 36 - 42
  • [9] NANO-SCALE DENSITOMETRIC QUANTITATION OF PHOSPHOLIPIDS
    HEDEGAARD, E
    JENSEN, B
    [J]. JOURNAL OF CHROMATOGRAPHY, 1981, 225 (02): : 450 - 454
  • [10] Hemker HC, 2000, THROMB HAEMOSTASIS, V84, P747